The Human Phenotype Ontology (HPO) provides the following list of features that have been reported in people with this condition. Much of the information in the HPO comes from Orphanet, a European rare disease database. If available, the list includes a rough estimate of how common a feature is (its frequency). Frequencies are based on a specific study and may not be representative of all studies. You can use the MedlinePlus Medical Dictionary for definitions of the terms below.
|Signs and Symptoms||Approximate number of patients (when available)|
|Stage 5 chronic kidney disease||5%|
|Autosomal dominant inheritance||-|
|Distal lower limb amyotrophy||-|
|Distal muscle weakness||-|
|Distal sensory impairment||-|
|Distal upper limb amyotrophy||-|
|Focal segmental glomerulosclerosis||-|
|Foot dorsiflexor weakness||-|
|Onion bulb formation||-|
Living with a genetic or rare disease can impact the daily lives of patients and families. These resources can help families navigate various aspects of living with a rare disease.
These resources provide more information about this condition or associated symptoms. The in-depth resources contain medical and scientific language that may be hard to understand. You may want to review these resources with a medical professional.
The following diseases are related to Autosomal dominant intermediate Charcot-Marie-Tooth disease type E. If you have a question about any of these diseases, you can contact GARD.